Back
Tier-1 pharma brand, metro Hyderabad location, and mid-level (5+ years) requirement, but niche lab-informatics reduces applicant density.
Requires regulated pharma lab informatics, GxP/cGMP validation and instrument-integration expertise, limiting cross-industry transferability.
Mandatory 5+ years in regulated environments, validation frameworks, and specific lab systems make shortlisting highly strict.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Serve as primary liaison between business stakeholders and technical teams for lab instrument integration and digital quality projects.
Lead requirements lifecycle management including elicitation, documentation, validation support, and traceability for systems like Scitara DLX, Empower, BIOVIA.
Drive alignment of integration solutions with business objectives, regulatory compliance, and optimized lab workflows across global teams.
Bachelor’s degree in Engineering, Science, Computer Science, Information Systems, or related discipline.
5+ years as Business Analyst in regulated environments such as pharmaceutical, life sciences, or manufacturing.
Experience working within SDLC and validation frameworks (GxP, cGMP).
Strong domain knowledge of lab operations, quality systems, or laboratory informatics.
Experienced in managing complex, cross-system lab instrument integration projects in global, matrixed organizations.
Skilled at translating complex business and regulatory requirements into actionable, testable deliverables supporting digital lab transformation.
Demonstrates ability to influence and collaborate across stakeholders and technical teams to improve compliance, workflows, and data integrity.